单细胞转录组学鉴定HNSCC免疫治疗反应的新预后特征。

IF 4.3 2区 医学 Q1 Medicine
Cancer Science Pub Date : 2025-08-12 DOI:10.1111/cas.70171
Kankui Wu, Xiuzhen Chen, Qiaobin Wu, Bin Liu, Fei Peng, Na Zhang, Yinhong Li, Jing Meng, Mingyu Liu
{"title":"单细胞转录组学鉴定HNSCC免疫治疗反应的新预后特征。","authors":"Kankui Wu, Xiuzhen Chen, Qiaobin Wu, Bin Liu, Fei Peng, Na Zhang, Yinhong Li, Jing Meng, Mingyu Liu","doi":"10.1111/cas.70171","DOIUrl":null,"url":null,"abstract":"<p><p>Head and neck squamous cell carcinoma (HNSCC) poses a major therapeutic challenge. In this study, we aimed to analyze tumor immune microenvironment changes and develop a prognostic model based on immunotherapy response. We analyzed single-cell RNA sequencing data from three HNSCC patients receiving TLR8 agonist and anti-PD1 combination therapy, identified cell subpopulations before and after treatment with a focus on six major immune cell types, and developed a LASSO-Cox risk stratification model using combined single-cell and bulk RNA sequencing data. We identified 19 pre-treatment and 13 post-treatment cell subpopulations. Analysis of six major immune cell types revealed differential gene expression patterns. Based on treatment-induced differential genes, we developed a LASSO-Cox model with 51 survival-associated genes, which showed robust predictive performance (AUC: 0.749-0.800) across different timepoints for both HPV-positive and HPV-negative patients. High-risk groups had elevated MDSCs and CAFs, decreased immune cell infiltration (except Th2 CD4+ T cells and common lymphoid progenitors), and increased expression of ICB-related genes. In conclusion, our model effectively captures patients' immune status and provides insights for optimizing HNSCC immunotherapy strategies.</p>","PeriodicalId":48943,"journal":{"name":"Cancer Science","volume":" ","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2025-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Single-Cell Transcriptomics Identifies Novel Prognostic Signatures in HNSCC Immunotherapy Response.\",\"authors\":\"Kankui Wu, Xiuzhen Chen, Qiaobin Wu, Bin Liu, Fei Peng, Na Zhang, Yinhong Li, Jing Meng, Mingyu Liu\",\"doi\":\"10.1111/cas.70171\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Head and neck squamous cell carcinoma (HNSCC) poses a major therapeutic challenge. In this study, we aimed to analyze tumor immune microenvironment changes and develop a prognostic model based on immunotherapy response. We analyzed single-cell RNA sequencing data from three HNSCC patients receiving TLR8 agonist and anti-PD1 combination therapy, identified cell subpopulations before and after treatment with a focus on six major immune cell types, and developed a LASSO-Cox risk stratification model using combined single-cell and bulk RNA sequencing data. We identified 19 pre-treatment and 13 post-treatment cell subpopulations. Analysis of six major immune cell types revealed differential gene expression patterns. Based on treatment-induced differential genes, we developed a LASSO-Cox model with 51 survival-associated genes, which showed robust predictive performance (AUC: 0.749-0.800) across different timepoints for both HPV-positive and HPV-negative patients. High-risk groups had elevated MDSCs and CAFs, decreased immune cell infiltration (except Th2 CD4+ T cells and common lymphoid progenitors), and increased expression of ICB-related genes. In conclusion, our model effectively captures patients' immune status and provides insights for optimizing HNSCC immunotherapy strategies.</p>\",\"PeriodicalId\":48943,\"journal\":{\"name\":\"Cancer Science\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2025-08-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cancer Science\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1111/cas.70171\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer Science","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/cas.70171","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

摘要

头颈部鳞状细胞癌(HNSCC)是一个主要的治疗挑战。在本研究中,我们旨在分析肿瘤免疫微环境的变化,并建立基于免疫治疗反应的预后模型。我们分析了三名接受TLR8激动剂和抗pd1联合治疗的HNSCC患者的单细胞RNA测序数据,确定了治疗前后的细胞亚群,重点关注六种主要免疫细胞类型,并利用单细胞和大量RNA测序数据建立了LASSO-Cox风险分层模型。我们鉴定了19个治疗前和13个治疗后的细胞亚群。对六种主要免疫细胞类型的分析揭示了不同的基因表达模式。基于治疗诱导的差异基因,我们建立了包含51个生存相关基因的LASSO-Cox模型,该模型在hpv阳性和hpv阴性患者的不同时间点显示出强大的预测性能(AUC: 0.749-0.800)。高危组MDSCs和CAFs升高,免疫细胞浸润减少(Th2 CD4+ T细胞和普通淋巴样祖细胞除外),icb相关基因表达增加。总之,我们的模型有效地捕获了患者的免疫状态,并为优化HNSCC免疫治疗策略提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Single-Cell Transcriptomics Identifies Novel Prognostic Signatures in HNSCC Immunotherapy Response.

Head and neck squamous cell carcinoma (HNSCC) poses a major therapeutic challenge. In this study, we aimed to analyze tumor immune microenvironment changes and develop a prognostic model based on immunotherapy response. We analyzed single-cell RNA sequencing data from three HNSCC patients receiving TLR8 agonist and anti-PD1 combination therapy, identified cell subpopulations before and after treatment with a focus on six major immune cell types, and developed a LASSO-Cox risk stratification model using combined single-cell and bulk RNA sequencing data. We identified 19 pre-treatment and 13 post-treatment cell subpopulations. Analysis of six major immune cell types revealed differential gene expression patterns. Based on treatment-induced differential genes, we developed a LASSO-Cox model with 51 survival-associated genes, which showed robust predictive performance (AUC: 0.749-0.800) across different timepoints for both HPV-positive and HPV-negative patients. High-risk groups had elevated MDSCs and CAFs, decreased immune cell infiltration (except Th2 CD4+ T cells and common lymphoid progenitors), and increased expression of ICB-related genes. In conclusion, our model effectively captures patients' immune status and provides insights for optimizing HNSCC immunotherapy strategies.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Cancer Science
Cancer Science ONCOLOGY-
CiteScore
9.90
自引率
3.50%
发文量
406
审稿时长
17 weeks
期刊介绍: Cancer Science (formerly Japanese Journal of Cancer Research) is a monthly publication of the Japanese Cancer Association. First published in 1907, the Journal continues to publish original articles, editorials, and letters to the editor, describing original research in the fields of basic, translational and clinical cancer research. The Journal also accepts reports and case reports. Cancer Science aims to present highly significant and timely findings that have a significant clinical impact on oncologists or that may alter the disease concept of a tumor. The Journal will not publish case reports that describe a rare tumor or condition without new findings to be added to previous reports; combination of different tumors without new suggestive findings for oncological research; remarkable effect of already known treatments without suggestive data to explain the exceptional result. Review articles may also be published.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信